Canonical Allele Identifier: PA2826562482
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376584
ClinVar RCV Id: RCV000418020 RCV000420225 RCV000420853 RCV000425483 RCV000424757 RCV000426139 RCV000431136 RCV000430390 RCV000432909 RCV000433579 RCV000435695 RCV000435015 RCV000440640 RCV000441393 RCV000442259 RCV000443110 RCV001183954 RCV002521507 RCV004022208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Cys116Arg
CA16603008
NM_001276697.3:c.346T>C